“…All the work performed on actinide-rich natural phases can explain why apatite ceramics have been synthesized in laboratories and studied as potential waste forms for high-level nuclear waste, particularly for actinide-rich waste streams [30,31,32,33]. For instance, the effects (amorphization, swelling) of both internal radiation by 244 Cmdoping [14,34,35,36,37,38,39,40] and external irradiation with heavy ions [14,33,41,42,43,44] (with energies around a few MeV) or -particles [42,45] have been studied for purely silicate apatites such as Ca2RE8(SiO4)6O2. Their crystalline structure exhibits hexagonal symmetry (space group P63/m) and consists of isolated SiO4 tetrahedra also referred to as Q 0 units (there is no bridging oxygen atom (BO) connecting two tetrahedra) with the Ca 2+ and RE 3+ cations located in two sites in which actinides may also enter [46,47,48] : a 7-fold coordinated site (6h site) that is preferentially occupied by RE 3+ cations surrounded by six oxygen atoms linked to SiO4 tetrahedra and one isolated oxygen anion and a 9-fold coordinated site (4f site) surrounded by nine oxygen atoms linked to SiO4 tetrahedra.…”